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Alexandra Schrader

dblp:99/9983 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2011
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.112011
Genomic data integration using guided clustering · Bioinform. 2011
Bioinformatics and computational biology › multi-omics data integration
genomic data integration
0.112011
Genomic data integration using guided clustering · Bioinform. 2011
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112011
Genomic data integration using guided clustering · Bioinform. 2011
Bioinformatics and computational biology
supervised clustering
0.112011
Genomic data integration using guided clustering · Bioinform. 2011

Methods — techniques the papers use, named apart from their topics

statistical simulation · 0.1clustering · 0.1
YearPublicationVenuePosition
2011 Genomic data integration using guided clustering
abstract
MOTIVATION: In biomedical research transcriptomic, proteomic or metabolomic profiles of patient samples are often combined with genomic profiles from experiments in cell lines or animal models. Integrating experimental data with patient data is still a challenging task due to the lack of tailored statistical tools. RESULTS: Here we introduce guided clustering, a new data integration strategy that combines experimental and clinical high-throughput data. Guided clustering identifies sets of genes that stand out in experimental data while at the same time display coherent expression in clinical data. We report on two potential applications: The integration of clinical microarray data with (i) genome-wide chromatin immunoprecipitation assays and (ii) with cell perturbation assays. Unlike other analysis strategies, guided clustering does not analyze the two datasets sequentially but instead in a single joint analysis. In a simulation study and in several biological applications, guided clustering performs favorably when compared with sequential analysis approaches. AVAILABILITY: Guided clustering is available as a R-package from http://compdiag.uni-regensburg.de/software/guidedClustering.shtml. Documented R code of all our analysis is included in the Supplementary Materials. All newly generated data are available at the GEO database (GSE29700). CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Matthias Maneck, Alexandra Schrader, Dieter Kube, Rainer Spang
Bioinform.2